Method for extracting quercitrin and bergenin
A technology of leucogenin and quercitrin, applied in the field of natural products, can solve the problems of low price, lack of chemical composition and pharmacological research of Sifangtan, and achieve the effects of shortening extraction time, reducing production cost and improving utilization rate
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Embodiment 1
[0027] Crush 100kg of vine to 90 mesh, add 15L of yeast liquid, ferment at room temperature for 3 days, add 300L of ether for reflux extraction at 55°C for 1 hour, and filter to obtain filtrate I and filter residue I. Add filter residue I to 10L of Trichoderma fermentation broth, ferment at 30°C for 20 hours, then add 10L of yeast liquid to it, ferment at 30°C for 4 days, then add 300L of 75% ethanol solution, carry out reflux extraction at 80°C for 1 hour, and filter to obtain filtrate II . Concentrate the filtrate I to obtain 4L concentrate I, concentrate the filtrate II to obtain 4L concentrate II, then combine the concentrate I and concentrate II, and then add 30L diethyl ether for extraction to obtain 35L extract I and 3L extract II. After the extract II was mixed evenly with 3L methanol, it was loaded on the LSA-8B macroporous resin column, and eluted with 80% methanol solution containing five times the column volume to obtain 120L eluent I. The extract I was concentrat...
Embodiment 2
[0033] Crush 200kg of vine to 100 mesh, add 25L of yeast liquid, ferment at room temperature for 3 days, add 550L of ether for reflux extraction at 55°C for 1 hour, and filter to obtain filtrate I and filter residue I. Add filter residue I to 30L of Trichoderma fermentation broth, ferment at 30°C for 20 hours, then add 20L of yeast liquid to it, ferment at 30°C for 4 days, then add 600L of 80% ethanol solution, carry out reflux extraction at 80°C for 1 hour, and filter to obtain filtrate II . Concentrate the filtrate I to obtain 7L concentrate I, concentrate the filtrate II to obtain 8L concentrate II, then combine the concentrate I and concentrate II, and then add 50L ether for extraction to obtain 58L extract I and 7L extract II. After the extract II was mixed evenly with 7L methanol, it was applied to a LSD-300 macroporous resin column, and elution was continued with six column volumes of 80% methanol solution to obtain 300L eluent I. Concentrate the extract Ⅰ to 1.5L, put...
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